[38F1-38F1];[39D2-39D2];
A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
38F1;39D2
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS3}CB-0690-3 and P{RS5}5-SZ-3556.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}Hr3802306&P{PZ}dia1 and P{EP}CG31673EP432 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k14505k14505&P{lacW}l(2)k05106k05106 and P{PZ}l(2)05095a05095a